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| Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction K Ozaki, Y Ohnishi, A Iida, A Sekine, R Yamada, T Tsunoda, H Sato, ... Nature genetics 32 (4), 650-654, 2002 | 1266 | 2002 |
| Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease K Yamazaki, D McGovern, J Ragoussis, M Paolucci, H Butler, D Jewell, ... Human molecular genetics 14 (22), 3499-3506, 2005 | 596 | 2005 |
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| Catalog of 605 single-nucleotide polymorphisms (snps) among 13 genes encoding human atp-binding cassette transporters: abca4, abca7, abca8, abcd1, abcd3, abcd4, abce1, abcf1 … A Iida, S Saito, A Sekine, C Mishima, Y Kitamura, K Kondo, S Harigae, ... Journal of human genetics 47 (6), 285-310, 2002 | 156 | 2002 |
| Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease K Yamazaki, M Takazoe, T Tanaka, T Ichimori, S Saito, A Iida, Y Onouchi, ... Journal of human genetics 49 (12), 664-668, 2004 | 154 | 2004 |
| A functional single nucleotide polymorphism in the core promoter region of CALM1 is associated with hip osteoarthritis in Japanese H Mototani, A Mabuchi, S Saito, M Fujioka, A Iida, Y Takatori, A Kotani, ... Human molecular genetics 14 (8), 1009-1017, 2005 | 152 | 2005 |
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| Mutations in B3GALT6, which encodes a glycosaminoglycan linker region enzyme, cause a spectrum of skeletal and connective tissue disorders M Nakajima, S Mizumoto, N Miyake, R Kogawa, A Iida, H Ito, H Kitoh, ... The American Journal of Human Genetics 92 (6), 927-934, 2013 | 140 | 2013 |
| A functional SNP in BNC2 is associated with adolescent idiopathic scoliosis Y Ogura, I Kou, S Miura, A Takahashi, L Xu, K Takeda, Y Takahashi, ... The American Journal of Human Genetics 97 (2), 337-342, 2015 | 139 | 2015 |
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| Molecular Strategy for Detecting Metastatic Cancers with Use of Multiple Tumor-specific MAGE-A Genes I Miyashiro, C Kuo, K Huynh, A Iida, D Morton, A Bilchik, A Giuliano, ... Clinical Chemistry 47 (3), 505-512, 2001 | 123 | 2001 |
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| Single nucleotide polymorphisms in the gene encoding Krüppel-like factor 7 are associated with type 2 diabetes A Kanazawa, Y Kawamura, A Sekine, A Iida, T Tsunoda, A Kashiwagi, ... Diabetologia 48, 1315-1322, 2005 | 108 | 2005 |
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| Three hundred twenty-six genetic variations in genes encoding nine members of ATP-binding cassette, subfamily B (ABCB/MDR/TAP), in the Japanese population S Saito, A Iida, A Sekine, Y Miura, C Ogawa, S Kawauchi, S Higuchi, ... Journal of human genetics 47 (1), 38-50, 2002 | 104 | 2002 |
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